Actively Recruiting

Phase Not Applicable
Age: 50Years - 74Years
All Genders
NCT06074536

Impact of Training Patient-centered Approach on Shared Decision in Colorectal Cancer Screening

Led by CNGE Conseil · Updated on 2026-02-11

400

Participants Needed

1

Research Sites

194 weeks

Total Duration

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AI-Summary

What this Trial Is About

The purpose of this study is to compare the effect of face-to-face training of general practitioners on the implementation of a shared decision (in the context of colorectal cancer screening), versus current practice (i.e. without training in the patient-centered approach).

CONDITIONS

Official Title

Impact of Training Patient-centered Approach on Shared Decision in Colorectal Cancer Screening

Who Can Participate

Age: 50Years - 74Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient aged 50 to 74
  • Eligible for organized colorectal cancer screening
  • Has a general practitioner investigator of the study as attending clinician
  • Consulting their attending clinician during the study
  • Able and willing to comply with all trial requirements
Not Eligible

You will not qualify if you...

  • Had colorectal cancer screening less than 2 years ago
  • Not eligible for organized colorectal cancer screening
  • Family history of adenomas or colorectal cancer in first-degree relatives
  • Personal history of inflammatory bowel disease including Crohn's disease or ulcerative colitis
  • Hereditary predispositions such as familial adenomatous polyposis or Lynch syndrome
  • Presence of symptoms requiring colonoscopy
  • Illiteracy preventing completion of self-questionnaire
  • Inability to give express consent
  • Under guardianship, curatorship, or having cognitive disorders

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Cabinet de groupe pluriprofessionnel

Soisy-sous-Montmorency, France, 95230

Actively Recruiting

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Research Team

I

Isabelle AUGER-AUBIN, Pr

CONTACT

J

Josselin LeBel, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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